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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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Ulrike Amann-Gassner

Project Manager

Ulrike Amann-Gassner holds a Diploma in Nutritional Sciences from Technical University of Munich and a PhD from University of Vienna.

Ulrike has more than 20 years of experience in managing clinical trials, NIS and PASS studies in a huge variety of indications as a CRA, lead CRA and Senior Project Manager in CROs, pharmaceutical companies and also from PII side.

During her scientific research time at TU Munich she was responsible for the working group of fetal programming and nutrition during pregnancy and lactation. She has a comprehensive list of publications in international recognized journals and presented her work at international conferences and meetings.

She joined ZEG in March 2023 and has the role of a Senior Project Manager in international PASS studies. She is also responsible for the scientific supervision and customer support of the Menopausal Rating Scale (MRS).

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Executive Team

  • Clare Barnett
  • Karl Pauls
  • Michael Schultze
  • Alfred Pauls
  • Do Minh Thai
  • Elisabeth Finger
  • Jens A. Lange
  • Antje Simon

Management Board

  • Klaas Heinemann
  • Clare Barnett
  • Marc Pignot
  • Karl Pauls
  • Johanna Poppe

Project Management Team

  • Pauline De Corte
  • Lisa Eggebrecht
  • Mohammed Dagher
  • Armin Papkalla
  • Silke Zimmermann
  • Nik Kolb

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ZEG Berlin

Berlin Center for Epidemiology and Health Research

Invalidenstraße 115
10115 Berlin
Germany

Contact Us

Expertise

  • Real-World Evidence
  • Non-interventional study design
  • Post-authorization safety studies
  • Post-authorization efficacy studies
  • Cohort studies
  • Case-control studies
  • Medical Devices
  • Patient Reported Outcomes (PROs)
  • Data collection instruments

Services

  • Crisis Management
  • Consulting
  • Data Management and Biostatistics
  • Medical Writing
  • Study Management
  • Quality Assurance
  • Pharmacovigilance

ENCePP

We are a partner centre of the ENCePP scientific network which is coordinated by the European Medicines Agency. We are dedicated to excellence in research by adhering to the ENCePP Guide on Methodological Standards and promoting scientific independence and transparency. We register studies in the ENCePP E-Register of Studies, a publicly accessible resource for the registration of pharmacoepidemiological and pharmacovigilance studies.

General Data Protection Regulation

With a view to the introduction of the GDPR/EUDSGVO we are glad to present our newupdated privacy policy . The updated description are stored under “about us” and then “privacy policy/GDPR”. Further translation for study participants will follow contemporary.

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